Does PEGFILGRASTIM Cause Drug dose omission? 2,089 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,089 reports of Drug dose omission have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 2.6% of all adverse event reports for PEGFILGRASTIM.
2,089
Reports of Drug dose omission with PEGFILGRASTIM
2.6%
of all PEGFILGRASTIM reports
3
Deaths
52
Hospitalizations
How Dangerous Is Drug dose omission From PEGFILGRASTIM?
Of the 2,089 reports, 3 (0.1%) resulted in death, 52 (2.5%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 2,089 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM Cause?
Device adhesion issue (11,326)
Wrong technique in product usage process (10,217)
Unintentional medical device removal (8,882)
Device malfunction (6,818)
Device use error (6,001)
Device issue (5,071)
Accidental exposure to product (4,967)
Device occlusion (3,239)
Off label use (3,228)
Bone pain (2,266)
What Other Drugs Cause Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which PEGFILGRASTIM Alternatives Have Lower Drug dose omission Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA